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Generic Name: tramadol hydrochloride
Summary for Generic Name: tramadol hydrochloride
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Clinical Trials for: tramadol hydrochloridePhase 3 Study of Tramadol Hydrochloride/Acetaminophen SR Tab. & Tramadol Hydrochloride/Acetaminophen Tab. in Low Back Pain Patients Status: Completed Condition: Low Back Pain A Study Comparing the Effectiveness and Safety of Extended Release (ER) Tramadol Hydrochloride (HCl)/Acetaminophen With Immediate Release (IR) Tramadol HCl/Acetaminophen in Participants With Moderate to Severe Postoperative Pain Status: Completed Condition: Pain, Postoperative Intraoperative Use of Dexketoprofen Trometamol, Pethidine Hcl, Tramadol Hcl and Their Combinations for Postoperative Pain Management in Laparoscopic Nissen Fundoplication Status: Active, not recruiting Condition: Laparoscopic Nissen Fundoplication A Comparison of the Analgesic Efficacy and Safety of Once Daily Tramadol HCl / Contramid® Tablets to Twice Daily Tramadol HCl (SR) for the Treatment of Osteoarthritis of the Knee Status: Completed Condition: Osteoarthritis, Knee; Pain A Study to Compare the Bioavailability of Two Tramadol Hydrochloride Tablet Products (50 mg and 200 mg, Respectively) at Steady-state Under Fasting Conditions Status: Completed Condition: Healthy Subjects; Pharmacokinetics; Bioavailability A Comparison of the Effectiveness and Safety of ULTRACET® (Tramadol Hydrochloride/Acetaminophen) Versus ULTRAM® (Tramadol Hydrochloride) Versus Placebo in Patients With Pain After Oral Surgery Status: Completed Condition: Surgery, Oral; Pain, Postoperative An Efficacy and Safety Study of Tramadol Hydrochloride-Paracetamol in Treatment of Moderate to Severe Acute Neck-Shoulder Pain and Low Back Pain Status: Completed Condition: Low Back Pain; Shoulder Pain; Neck Pain A Study to Compare the Relative Bioavailability of Two 200 Mg Tramadol Hydrochloride Tablet Products Under Fasting Conditions Status: Completed Condition: Healthy An Open Label Study to Evaluate Safety, Tolerability and Clinical Utility of ULTRACET® (37.5mg Tramadol Hydrochloride/325mg Acetaminophen) for the Treatment of Breakthrough Pain in Cancer Patients Status: Completed Condition: Pain A Study to Assess the Improvement of Pain and Health-Related Quality of Life in Patients With Chronic Non-Malignant Pain Taking Tramadol Hydrochloride and Acetaminophen Status: Completed Condition: Chronic Pain Courtesy of ClinicalTrials.org See more clinical trials for this drug | |||||||||||||||
Glossary
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Type | RLD | Patent No. | Product | Substance | Delist_Flag | Patent Expiration | Patented / Exclusive Use | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Janssen Pharms | ULTRAM | tramadol hydrochloride | TABLET; ORAL | 020281 | Mar 3, 1995 | RX | Yes | 6,339,105*PED | Y | <disabled> | A TITRATION DOSING REGIMEN FOR THE TREATMENT OF PAIN USING AN INITIAL DOSE OF ABOUT 25MG | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Janssen Pharms | ULTRAM | tramadol hydrochloride | TABLET; ORAL | 020281 | Mar 3, 1995 | DISCN | No | 6,339,105*PED | Y | <disabled> | A TITRATION DOSING REGIMEN FOR THE TREATMENT OF PAIN USING AN INITIAL DOSE OF ABOUT 25MG | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Zydus Pharms Usa Inc | TRAMADOL HYDROCHLORIDE | tramadol hydrochloride | TABLET; ORAL | 090404 | Jan 31, 2011 | RX | No | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Watson Labs | TRAMADOL HYDROCHLORIDE | tramadol hydrochloride | TABLET; ORAL | 075962 | Jun 24, 2002 | RX | No | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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